| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:113086238-113086598 | Common:11; Rare:99 | ||||
| chr7:114085708-114085892 | Common:1; Rare:39 | ||||
| chr7:114086205-114086568 | Common:2; Rare:136 | ||||
| chr7:114087606-114087766 | Common:1; Rare:41 | ||||
| chr7:114414233-114414253 | Rare:2 | ||||
| chr7:114414741-114415067 | Common:3; Rare:68; Clinvar:1 | ||||
| chr7:114416258-114416404 | Rare:27 | ||||
| chr7:114426320-114426678 | Rare:102; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:116210413-116210629 | Common:3; Rare:57 | ||||
| chr7:116862351-116862650 | Common:2; Rare:106 | ||||
| chr7:117020074-117020446 | Common:3; Rare:61 | ||||
| chr7:117872174-117872444 | Common:3; Rare:51 | ||||
| chr7:117873418-117873638 | Common:1; Rare:77 | ||||
| chr7:118183964-118184217 | Common:2; Rare:100 | ||||
| chr7:118214557-118214735 | Common:2; Rare:62 |